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Article

A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14.

Neurology - 24 Dec 2002

Hodgkinson C A, Bohlega S, Abu-Amero S N, Cupler E, Kambouris M, Meyer B F, Bharucha V A

Abstract excerpt

BACKGROUND: Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous disorder characterized by a progressive weakening and spasticity of the lower limbs. HSP is classified according to the presence or absence of accompanying neurologic problems and by the mode of inheritance. Currently, 17 loci have been linked to the various forms of HSP. OBJECTIVE: To determine the chromosomal location...

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Share to Chromosomes, Human, Pair 13

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 12499481
DOI: 10.1212/01.wnl.0000036909.49629.21

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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